Yan Jiayu, Zhang Jianguo, Pang Wenbo, Peng Chunhui, Chen Yajun
Department of General Surgery, Beijing Children's Hospital, Capital Medical University, National Center for Children's Health, No. 56 Nalishi Road, Xicheng District, Beijing, 100045, China.
Department of Pediatric Surgery, Inner Mongolia Maternal and Child Health Care Hospital, Hohhot, 010020, China.
Pediatr Surg Int. 2025 Jun 13;41(1):168. doi: 10.1007/s00383-025-06071-1.
To summarize the clinical features and surgical treatments of patients with total colonic duplication (TCD).
Clinical data on 7 TCD patients who underwent surgical treatments at Beijing Children's Hospital from January 2010 to December 2024 was retrospectively collected and analyzed, including clinical presentations, surgical details, and prognosis.
Of the 7 patients, 4 (57%) were female. In addition to 1 patient whose prenatal ultrasound revealed abnormalities, abnormalities were found in all patients after birth, including 3 passing meconium through the fossa vestibuli vaginae, 2 with constipation/vomiting, 1 with cloaca, and 1 passing meconium through the urethra. Of the 7 patients, 2 were accurately diagnosed and treated in time (the patient with cloaca who underwent colostomy and the patient who was examined in our outpatient department after birth), and 5 (71%) were not. The average age at hospitalization was 14 (6-138) months. Before hospitalization, 4 patients (57%) experienced rectal mass prolapse during defecation. All patients underwent laparotomy, including 5 undergoing the "distal cross-section, mucosa stripping and closure" procedure, 1 resection of the distal duplicated colon with the proximal end closed and ileostomy, and 1 Soave procedure and ileostomy. All patients recovered well without fecal incontinence except for the patient with cloaca who defecated more than 3 times per day.
In addition to abnormalities after birth, rectal mass prolapse may be a specific presentation of TCD. The aim of surgery for TCD is to connect the duplicated and native colon and ligate the fistula.
总结全结肠重复畸形(TCD)患者的临床特征及外科治疗方法。
回顾性收集并分析2010年1月至2024年12月在北京儿童医院接受手术治疗的7例TCD患者的临床资料,包括临床表现、手术细节及预后情况。
7例患者中,4例(57%)为女性。除1例产前超声检查发现异常外,其余患者均于出生后发现异常,包括3例经前庭窝排胎粪、2例便秘/呕吐、1例泄殖腔畸形、1例经尿道排胎粪。7例患者中,2例得到准确诊断并及时治疗(泄殖腔畸形患者行结肠造口术,1例出生后在我院门诊检查的患者),5例(71%)未得到及时诊断。平均住院年龄为14(6 - 138)个月。住院前,4例患者(57%)排便时出现直肠肿物脱出。所有患者均接受剖腹手术,其中5例行“远端横断、黏膜剥除及闭合”手术,1例行远端重复结肠切除、近端闭合及回肠造口术,1例行Soave手术及回肠造口术。除泄殖腔畸形患者每天排便超过3次外,所有患者恢复良好,无大便失禁。
除出生后异常外,直肠肿物脱出可能是TCD的特异性表现。TCD手术的目的是将重复结肠与正常结肠连接并结扎瘘管。